Abnormality of iron homeostasis

Symptom Information:

Symptom ID: HPO:0011031
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormal hepatic iron concentration
HPO         Abnormality of transition element cation homeostasis
HPO         Abnormal serum iron
HPO         Abnormal serum ferritin
HPO         Abnormal transferrin saturation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of ion homeostasis(HPO:0003111)
             Abnormality of cation homeostasis(HPO:0010929)
                Abnormality of transition element cation homeostasis(HPO:0011030)
                   Abnormality of iron homeostasis(HPO:0011031)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Aceruloplasminemia (Orphanet:48818)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia intermedia (Orphanet:231222)
Beta-thalassemia major (Orphanet:231214)
GRACILE syndrome (Orphanet:53693)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hemoglobin E - beta-thalassemia (Orphanet:231249)
Neonatal hemochromatosis (Orphanet:446)
Neurodegeneration with brain iron accumulation (Orphanet:385)
Rare hereditary hemochromatosis (Orphanet:220489)
Syndromic diarrhea (Orphanet:84064)